EP0349532B1 - Thermisches aufzeichnungsmittel - Google Patents
Thermisches aufzeichnungsmittel Download PDFInfo
- Publication number
- EP0349532B1 EP0349532B1 EP88900435A EP88900435A EP0349532B1 EP 0349532 B1 EP0349532 B1 EP 0349532B1 EP 88900435 A EP88900435 A EP 88900435A EP 88900435 A EP88900435 A EP 88900435A EP 0349532 B1 EP0349532 B1 EP 0349532B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- thermal imaging
- image forming
- imaging medium
- layer
- forming substance
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
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- Y10T428/24901—Discontinuous or differential coating, impregnation or bond [e.g., artwork, printing, retouched photograph, etc.] including particulate material including coloring matter
Definitions
- the invention relates generally to a heat mode recording material and, more particularly, to a high resolution thermal imaging medium comprising a heat sensitive layer interacting, at an image-wise application of heat, with an image forming substance for producing images of very high resolution.
- thermal imaging media require neither a dark room nor any other protection from ambient light. Instead, images may be produced with thermal imaging media by the application of heat patterns corresponding to the image to be produced and, since these materials can provide images by quicker and simpler processes than those applicable to silver halide materials, they are more convenient and economical than conventional photographic imaging materials.
- thermal imaging media require substantially dry image developing processes and they are unaffected by sustained periods of elevated ambient temperatures.
- thermal imaging media allow the making of more stable images of higher quality because they do not suffer from the image quality drift resulting from the wet processing and temperature effects of silver halide materials.
- thermal imaging media may be used with relative ease and in a potentially wide range of applications, proposals relating to their manufacture and use have not been lacking.
- One source of heat lately to have become conventional for exposing thermal imaging media are lasers of sufficient power output and appropriately modulated while scanning a medium in an image pattern. The time required for irradiating the medium in this manner is relatively short.
- Other materials use conventional heat sources such as, for instance, xenon flash tubes.
- U.S Patent 4,123,309 discloses a composite strip material including an accepting tape comprising a layer of latent adhesive material in face-to-face contact with a layer of microgranules lightly adhered to a donor web. At least one of the layers bears a radiation absorbing pigment, such as carbon black or iron oxide, which when selectively heated in accordance with a pattern of radiation, momentarily softens adjacent portions of the adhesive material sufficiently for the latter completely to penetrate through the pigment.
- a radiation absorbing pigment such as carbon black or iron oxide
- U.S.Patent 4,157,412 discloses a composite material for forming graphics which includes a layer of latent adhesive material, a mono-layer of granules lightly adhered to a donor web, and a thin layer of bonding material between and in face-to-face contact with layers of granules and adhesive.
- the layer of bonding material maintains the adhesive and granular layers in close proximity and excludes air from therebetween.
- corresponding portions of the bonding layer melt and corresponding portions of the adhesive material and granular layer soften, absorb the melted portions of the bonding layer and adhere together.
- the remaining portions of the layer of bonding material separate, whereas granules transfer to the accepting tape in the heated areas to provide the graphics.
- a heat mode recording material which comprises a support and a heat sensitive layer positioned on the support, in which the heat sensitive layer comprises an ionomer resin obtained by ionically cross-linking with at least one metal ion, a copolymer comprising an alpha- olefin and an alpha methylene aliphatic monocarboxylic acid and a hydrophobias binder.
- thermal imaging materials None of the known thermal imaging materials appear to have found wide acceptance, possibly because of the relatively complicated mechanism of the image-wise transfer of an image-forming substance from a donor layer to a receiving layer as a result of applied heat patterns. Other problems may be involved in the coherence of the image-forming substance which may not consistently yield images of a resolution sufficiently fine to be acceptable to consumers. Still further problems may result from the difficulty of removing microscopical irregularities and air gaps when using two separate donor and receiver webs. It appears that none of the thermal imaging materials currently available satisfy the demand for high photographic quality or high resolution required by industry.
- Another object of the invention resides in the provision of a thermal imaging medium yielding images of improved density.
- a further object of the invention resides in the provision of a thermal imaging medium of improved sensitivity.
- Still another object resides in the provision of a thermal imaging medium of improved abrasion resistance.
- thermo imaging medium for forming images in response to intense image-forming radiation, comprising the combined features of claim 1.
- the material of the image forming surface is such that it has a narrow temperature range between liquefying and solidifying.
- thermal imaging is intended to connote producing an image of a subject by exposing a recording medium or material to an image-wise distribution of thermal energy.
- a method particularly preferred for providing the image-wise distribution involves the use of a laser capable of providing a beam sufficiently fine to yield an image of as fine a resolution as one thousand (1000) dots per cm.
- two steps are required to form an image in the thermal imaging medium in accordance with the present invention: one is proper heat exposure, the other is processing of the latent image by a process of removing from the medium those parts of an image forming substance which have not been exposed.
- the quality of the image thus obtained is a function of a reliably predictable interaction between these two variables.
- the source of heat utilized is a laser.
- the source of heat utilized for forming a latent image in the material will be assumed to be a laser, but it should be understood that the invention is not itself restricted to media for laser imaging.
- colorant/binder layer In the event, laser exposures cause very high temperatures to be generated in the medium, at the interface between an image forming surface and an image forming substance deposited on the image forming surface as a particulate or porous uniform layer, hereinafter referred to as colorant/binder layer.
- the temperature may be as high as 400 ° C, but it is achieved for a very brief period only, e.g. 0.1 microsecond. It is achieving such high temperatures which causes the particulate or porous layer to adhere to the image forming surface of the medium.
- an image may be formed by removing from the image forming surface those portions of the colorant/binder layer which have not been exposed. In preferred embodiments of the invention this may yield complementary "negative" and "positive" images.
- Models of the mechanism for connecting exposed portions of the colorant/binder layer to the image forming surface, and of the removal of unexposed portions, may be used, with empirical experimentation, as guides to optimizing the chemistry of the layers to supplement the exposure and processing steps. While no definite reasons have been found explaining the superior performance of the thermal imaging medium of the present invention, electron-microscopical measurements seem to support the conclusions set forth below.
- connection of the colorant/binder layer to the image forming surface may qualitatively be modelled on the Washburn equation for the rate of penetration of a liquid into a capillary.
- the pores of the particulate colorant/binder layer may be considered to constitute a plurality of capillaries; on the other hand, the image forming surface, when heated by the laser, may be assumed to act like a liquid, for polymeric materials of the kind here under consideration, when heated to about 400 °C are about as viscous as water at room temperature.
- the colorant/binder layer does not adhere to the image forming surface before laser heating because the viscosity of the unheated image forming surface is in excess of 10 13 Pa.s (10 14 poise). During laser heating the viscosity drops to about 0.001 Pa.s (0.01 poise). Hence, the velocity of the capillary meniscus moving into the particulate layer is sixteen orders of magnitude higher during laser heating than at room temperature. For practical purposes, the surface tension of most liquids may be assumed to decrease linearly with increasing temperature. When the medium in accordance with the invention is subjected, at least at the interface between the colorant/binder layer and the image forming surface, to a temperature of about 400 °C the resultant surface tension of the liquefied image forming surface is probably about zero.
- Capillary attraction occurs when the tension of adhesion, G 1 v Cos 0, exceeds zero. This is important. For the adhesion tension determines whether the image forming surface possesses capillary attraction in respect of the particulate or porous colorant/binder layer, once the viscosity of the image forming surface has been lowered under the impact of laser heating. While conflicting effects occur with an increase in temperature in that G 1 v approaches zero and cos 0 approaches one, it is nevertheless possible to generalize that (a) the adhesion tension cannot exceed G 1 v and (b) if the adhesion tension is less than zero capillary repulsion results.
- the adhesion tension of the medium of the invention is between 0 and 0.05 N/m (0 and 50 dynes/cm), and the viscosity of its image forming surface varies between less than 0.001 Pa.s ( 0 . 01 poise) and 10 13 Pa.s (10 14 poise), one may deduce from the Washburn equation that the enormous decrease in viscosity has rather greater an impact on the capillary penetration of the liquefied image forming surface into the particulate layer than the adhesion tension.
- the peeling process may qualitatively be modelled on a "plunger” analogy.
- the balance between the force acting to peel an unexposed spot in the colorant/binder layer off the image forming surface, and the sum of the cohesive and base adhesive forces of the colorant/binder layer determines whether or not removal of a spot will take place. That is to say, an isolated unexposed spot in an exposed area is not removed from the image forming surface if where Fp, Fb and Fc are, respectively, the force acting to peel the layer off the image forming surface, the force of adhesion of the layer to the image forming surface and the cohesive force of the layer.
- L is the thickness of the colorant/binder layer and r is the radius of the spot.
- the radius (r) of the spot For forming images of high resolution or photographic quality, the radius (r) of the spot must be very small. This produces a cohesive force ⁇ (2L/r)-Fc ⁇ which is very large, and may prevent removing small unexposed spots from the image forming surface.
- a colorant/binder layer with lower cohesion (Fc) and a small thickness (L) will reduce the cohesive force and allow removing small unexposed spots.
- low cohesion will result in splitting of the particulate layer, rather than in a clean transfer, during peeling. This prevents producing clean "positive” and "negative” images and makes the density of the obtainable image unpredictable.
- the cohesion of this layer must exceed either the adhesive or the peeling force (Fc > Fb or Fp).
- the cohesion and/or thickness of this layer must not exceed specific values determined by the desired resolution of the final image.
- the peeling force is dependent on the peeling temperature and the rate of peeling. While there may exist an ideal temperature related to an ideal peeling rate, the medium should offer parameters which allow producing satisfactory images under less than ideal circumstances.
- Exposing the medium by means of a laser is believed to increase Fb and/or decrease Fs. For instance, if the colorant/binder layer of the medium is covered by a heat activated release layer the heat generated by the laser exposure will decrease Fp, or if the image forming surface is heat activated the heat from the laser will increase Fb.
- Materials providing image forming surfaces and colorant/binder layers may be selected on the basis of the criteria set forth above.
- the great importance of viscosity requires selecting materials that display a catastrophic drop in viscosity with increasing temperature at high frequency or short periods.
- the frequency dependence of the viscosity at a given temperature is of great importance since the heat of the laser is only applied for about 10-'s (10 7 Hz).
- a thermal imaging material referred to as the medium, useful for practicing the invention and identified by reference numeral 10 in Fig. 1 basically comprises a first web 12 of polymeric material pervious to image forming radiation and having a substantially continuous smooth image forming surface 14 upon which there is uniformly deposited a uniformly thin particulate or porous colorant/binder layer 16 for forming images in the surface 14 of the web 12.
- the web 12 may be present in the form of an integral unit having a thickness of from about 1 to about 1000 am, or it may be laminated, either permanently or temporarily, to a subcoat, such as paper or another polymeric material, as a uniform layer of a thickness sufficient for purposes to be described.
- a subcoat such as paper or another polymeric material
- the web 12 is preferably made of a material which, when subjected to intense heat within a defined range of elevated temperatures at about 400 ° C, experiences a catastrophic change in viscosity, as from about 10 13 Pa.s (10 14 poise) at room temperature to about 10- 3 Pa.s (10- 2 poise) at the elevated temperature.
- the web 12 when subjected to radiation for liquefying its image forming surface 14 followed by a no less rapid cooling for solidifying the surface should be dimensionally stable in the sense that it neither expand nor contract in any dimension as a result of such vast changes in temperature.
- Materials suitable as webs 12 include polystyrene, polyethylene terephthalate, polyethylene, polypropylene, copolymers of styrene and acrylonitrile, polyvinyl chloride, polycarbonate and vinylidene chloride.
- polyethylene terephthalate as traded by E.I.du Font de Nemours & Co. under its tradename Mylar or by Eastman Kodak Company under its tradename Kodel is preferred.
- the layer 16 comprises an image forming substance deposited on the image forming surface 14 as a porous or particulate coating.
- the layer 16 may preferably be formed from a colorant dispersed in a binder, the colorant being a pigment of any desired color preferably substantially inert to the elevated temperatures required for image formation.
- Carbon black has been found to be of particular advantage. It may preferably have particles 18 of an average diameter of about 0.1 to 10 micrometers.
- other optically dense substances such as graphite, phthalocyanine pigments, and other colored pigments, may be used to equal advantage. It may even be possible to utilize substances which change their optical density when subjected to temperatures as herein described.
- the binder provides a matrix to form the pigment particles into a cohesive mass and serves initially physically to adhere the pigment/binder layer 16 in its dry state to the image forming surface 14 of the web 12.
- the ratio of pigment to binder may be in the range of from about 40 : 1 to about 1 : 2 on a weight basis. In a preferred embodiment the ratio is about 5 : 1.
- the carbon particles 18 may initially be suspended in a preferably inert liquid for spreading, in their suspended state, over the image forming surface 14. Thereafter, the layer 16 may be dried to adhere to the surface 14.
- the carbon may be treated with surfactants such as, for instance, ammonium perfluoroalkyl sulfonate.
- surfactants such as, for instance, ammonium perfluoroalkyl sulfonate.
- Other substances, such as emulsifiers may be used or added to improve the uniformity of distribution of the carbon in its suspended and, thereafter, in its spread dry states.
- the layer may range in thickness from about 0.1 to about 10 micrometers. Thinner layers are preferred because they tend to provide images of higher resolution.
- Gelatin polyvinyl alcohol, hydroxyethylcellulose, gum arabic, methylcellulose, polyvinylpyrrolidone, polyethyloxazoline and polystyrene latex are examples of binder materials suitable for use in the present invention.
- submicroscopic particles such as chitin and/or polyamide may be added to the colorant/binder layer 16 to provide abrasion resistance to the finished image.
- the particles may be present in amounts of from about 1 : 2 to about 1 : 20 , particles to layer solids, weight/weight basis. Polytetrafluoroethylene particles are particularly useful.
- the medium must be capable of absorbing energy at the wavelength of the exposing source at or near the interface of the web 12, i.e. the image forming surface 14, and the layer 16.
- the energy absorption characteristic may be inherent in the materials of either web 12 or layer 16 or it may be provided as a separate heat absorption layer.
- a laser beam schematically indicated by arrow 20, of a fineness corresponding to the desired high resolution of the image is directed to the interface between the colorant/binder layer 16 and the image forming surface 14, through the web 12.
- the beam 20 emanates from a laser schematically shown at 22 and is scanned across the image forming surface 14 in a pattern conforming to the image to be formed.
- the beam 20 is absorbed at the interface and is converted to heat measuring about 400 °C, although depending on the characteristics of the image forming surface 14, lower temperatures may also be effective for the purpose of forming an image.
- the image-wise scanning may be accomplished by linearly scanning the image forming surface 14 and modulating the laser 22, preferably in a binary fashion, to form the image by way of very fine dots in a manner not unlike half-tone printing.
- the laser 22 is preferably either a semiconductor diode laser or a YAG-laser and may have a power output sufficient to stay within upper and lower exposure threshold values of the imaging medium 10.
- the laser 22 may have a power output in the range of about 40 to about 1000 mW.
- Exposure threshold value connotes, on the one hand, the minimum power required to effect an exposure and, on the other, maximum power output tolerable to the imaging medium 10 before a "burn out" occurs.
- the laser 22 is equipped with focussing apparatus (not shown) for precisely focussing the laser beam.
- Lasers are particularly suitable for exposing the medium of the invention because the latter is intended as what may conveniently be termed a threshold type film. That is to say, it possesses high contrast and, if exposed beyond a certain threshold value, it will yield maximum density, whereas no density at all is obtained below this threshold.
- the intensity of a focussed Gaussian laser beam gradually decreases from a maximum in the center of the beam.
- dots written by a Gaussian laser beam would display a gradual decrease in density from their center towards their margin.
- the rate of decrease in density is sometimes referred to as the "gamma" of the medium.
- a low gamma medium would display spots of soft or gradual edges.
- high gamma media would write sharp spots with crisp edges.
- the medium in accordance with the present invention is such a high gamma medium in that edges are attainable which are sharper than those of the exposing laser beam.
- the written dots may be modulated to be either completely dark or completely clear, so that the density of an image formed in the image forming surface of media in accordance with the present invention may be varied by a half-tone technique in which increasing area and/or number of dark dots increase the density of that area. Images may, therefore, be created with the medium of the present invention which in quality resemble photographs.
- focussed laser beams cannot produce a uniformly intense spot, so that in the manner of the very common Gaussian beam spot, some areas of the film, i.e. the medium, may be considered to be well under and well over its exposure threshold.
- the web 12 be substantially non- absorptive of the wavelength of the laser, so that its beam may penetrate to the interface.
- the energy of the laser 22 is directed and penetrates through the web 12.
- birefringence of the support web 12 and of the image forming surface 14 must be taken into consideration when focussing lasers to small spots. If the spot is too small, e.g. ⁇ 5 am, support of the materials of these elements may cause distortion of the spot shape and loss of resolution and sensitivity.
- either the surface zone 14 or the particulate layer 16 must be heat absorptive or include a heat absorbing material.
- a heat absorbing material For instance, infrared absorbing layers have been found to be useful in this respect.
- carbon black being itself an excellent heat absorbing material, it may not be necessary or economical to provide a special layer.
- the intense (about 400 °C) and locally applied heat developed at the interface between the image forming surface 14 and the particulate layer 16 causes the surface 14, where it is subjected to the heat, to liquefy, i.e. experience a catastrophic drop in viscosity from about 10 13 Pa.s (10 14 poise) to about 10- 3 Pa.s (10- 2 poise).
- the heat is applied for an extremely short period, preferably in the order of ⁇ 0.5 microseconds, and causes liquefactions of the material to a depth of about 0.1 micrometer (see FIG. 12).
- the liquefied material exhibits capillary action with respect to the carbon black particles 18 of the layer 16 sufficiently to penetrate voids between the particles 18 without totally absorbing them. It is believed that the limited penetration of the liquefied surface material into the voids between the carbon black particles 18 is responsible for the fine resolution of images attainable with media of the present invention.
- the exposure time span may be ⁇ 1 msec and the temperature span may be between about 100 ° C and about 1000°C.
- a sheet 24 having a surface 26 covered with a pressure sensitive adhesive may be superposed on the particulate layer 16, and may then be removed or peeled off in the manner indicated by an arrow 28 (see FIG. 2).
- the sheet 24 As the sheet 24 is removed, it carries with it those portions (see 16 c u in Fig. 7) of the particulate layer 16 which were not subjected to the heat of the laser 22.
- the portions designated 16 c t treated by the laser beam 22 remain firmly attached to the surface 14 c in form of what for the sake of convenience may be called a "negative" image, the parts 16 c u removed with the sheet 24 c forming a complementary or "positive" image.
- the particulate layer 16 possess an inherent cohesion greater than its adhesion to the stripping sheet 24 and the web 12.
- the particulate layer 16 spread upon the surface 14 of the web 12 preferably adheres thereto, at least initially, in a manner precluding its accidental dislocation. While, as indicated supra, the particulate layer 16 may be provided with a matrix, it has been found that carbon black applied to the surface 14 in powder form, without any binding agent, will connect to the surface 14 in the manner of this invention after treatment with a heat source. The untreated carbon black may then be removed by rubbing or washing or the like instead of, as in the above embodiment, by an adhesive strip sheet 24.
- the medium 10a may be a laminate structure comprising a web 12a having an image forming surface 14a, a porous or particulate image forming layer 16a positioned on the surface 14a, a stripping or peeling sheet 24a, and a release layer 24a' in contact with the particulate layer 16a and deposited on the stripping sheet 24a.
- the particulate matter 18a forming the colorant/binder layer is positioned on the image forming surface 14a and does not penetrate into it.
- the thermal imaging medium 10a may be exposed by a laser beam 20a (see Fig. 3) in the manner previously described. Thereafter, the stripping sheet 24a may be removed carrying with it those portions 16a of the particulate colorant layer 16a which have not been treated by the laser beam 20a. The treated portions 16a will remain, firmly connected to the image forming surface 14a, on the web 12a.
- the particulate matter 18a is now slightly recessed into the image forming surface 14a as a result of the capillary attraction between the liquefied surface material and the colorant/binder layer 16a, in the manner explained above.
- the medium 10b comprises a web 12b preferably made of polyethylene terephthalate (Mylar) with a subcoat 12b' made of polystyrene or styreneacrylonitrile (SAN). Placed on the subcoat 12b' and in contact with an image forming surface 14b thereof is a particulate or porous colorant/ binder layer 16b comprising carbon black and polyvinylalcohol.
- a release coat 24b' made of a microcrystalline wax emulsion (Michelman 160) is placed over the colorant/binder layer 16b.
- the release coat 24b' is in turn covered by a stripping sheet 24b made of carboxylated ethylenevinylacetate and polyvinylacetate (Airflex 416 and Daratak 61 L). Finally, a web 24b" of paper coated with an emulsion of ethylene-vinylacetate (Airflex 400) is coated over the stripping sheet 24b.
- the medium 10b is preferably exposed by a laser beam 20b directed through the web 12b to generate heat at the interface between the colorant/binder layer 16b and the surface 14b of the web 12b.
- a heat absorption layer, such as an IR-absorber, may additionally be provided to direct the effect of the laser beam to a predetermined location in the laminate structure of the medium 10b.
- the relative adhesive strengths between the several layers of the laminate medium 10b are such that before exposure separation would occur between the subcoat 12b' and the colorant/binder layer 16b, whereas after exposure the separation would occur between or within the release coat 24b' and the stripping sheet 24b.
- FIG. 6 Another embodiment of the medium 10c is shown in Fig. 6.
- This embodiment comprises a web 12c covered by a colorant/binder layer 16c, which in turn is covered by a stripping sheet 24c. Exposure of the medium 10c is accomplished by a laser beam 20c directed through the web 12c to generate heat in the manner described above at the interface between the colorant/binder layer 16c and the web surface 14c, in the preferred method through the web 12c provided on the stripping sheet 24c.
- a carbon black solution was prepared from 4.25g carbon black solution (43% solids) (sold under the tradename Flexiverse Black CFD-4343 by Sun Chemical Co.)
- a carbon black solution containing no polymeric binder or FLUORAD surfactant was prepared from
- the unexposed carbon black coated web from Example I was coated with a release layer from a solution consisting of:
- Example III Another structure was prepared as in Example III but with the wax emulsion replaced by a polyethylene aqueous wax emulsion (sold under the tradename Jonwax 26 by S.C.Johnson and Son, Inc.) at the same concentration and coverage
- Example III Another structure was prepared as in Example III but the Mylar surface was first coated with 2g/m 2 of styrene acrylonitrile copolymer.
- the unexposed carbon black coated web of Example III was laminated at about 75 °C to a second Mylar web of 0.1 mm thickness.
- the laminated structure was exposed through the carbon black coated web of Example III by a laser beam of 0.1 J/cm 2 for 1 microsecond. After exposure the laminate was peeled apart to produce one negative and one positive image.
- the negative image consisted of exposed carbon black firmly connected to the surface of the web of Example III.
- the positive image consisted of unexposed carbon black adhered to the surface of the stripping layer, the latter being adhered to the surface of the second Mylar web.
- the stripping layer was then peeled from the second Mylar web so the latter could be used again for another lamination and peeling.
- Example IV The second Mylar web of Example IV, prior to lamination, was coated with an adhesive solution consisting of ethylenevinylacetate copolymer emulsion (52% solids) (sold under the tradename Airflex 400 by Air Products and Chemicals, Inc.) to give a dry coverage of about 5g/m 2.
- the unexposed carbon black coated web from Example III was laminated at about 70 ° C to this second Mylar web with the adhesive coating of this example in face-to-face contact with the stripping layer of Example III. The laminate was exposed and processed as in Example IV.
- the laminate was peeled apart to produce one negative and one positive image.
- the stripping layer could not be peeled from the second Mylar web. This example was repeated with a paper second web instead of Mylar to produce a reflection image in this web instead of a transparency.
- the second web of this example was heated after the peeling step to a temperature above the melting point of the wax release layer (about 90 ° C). This improved the durability of the image by allowing the melted wax to flow into the porous carbon black layer.
- the stripping layer surface of the unexposed carbon black containing web from Example III was overcoated with a 40% aqueous solution of polyethyloxazoline (as in Example I) to give a dry coverage of about 10g/m 2.
- This dried layer was then overcoated with a solution containing equal amounts of a 20% aqueous solution of polyethyloxazoline and a 27.5% aqueous solution of titanium dioxide to give a dry coverage of about 10g/m 2 .
- This structure was then exposed and peeled as in Example III to produce two images, the first being a negative carbon black image firmly connected to the surface of the Mylar web in areas of laser exposure.
- the second image was a positive reflection print image consisting of unexposed carbon black adhered to the surface of the stripping layer.
- the unexposed carbon black coated web from Example III was coated with a release layer from a solution of
- magenta pigment toner sold under the tradename Spectra Magenta Toner by Sage Co.
- the toned positive image was then washed with soapy water to remove the unexposed carbon black and leave a negative magenta image on the transparent adhesive tape.
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- Physics & Mathematics (AREA)
- Optics & Photonics (AREA)
- Thermal Transfer Or Thermal Recording In General (AREA)
- Heat Sensitive Colour Forming Recording (AREA)
- Laminated Bodies (AREA)
- Optical Record Carriers And Manufacture Thereof (AREA)
- Transforming Light Signals Into Electric Signals (AREA)
- Image-Pickup Tubes, Image-Amplification Tubes, And Storage Tubes (AREA)
- Developing Agents For Electrophotography (AREA)
- Investigating Or Analyzing Materials Using Thermal Means (AREA)
- Solid State Image Pick-Up Elements (AREA)
Claims (31)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
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AT88900435T ATE97613T1 (de) | 1986-12-09 | 1987-12-07 | Thermisches aufzeichnungsmittel. |
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
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US93985486A | 1986-12-09 | 1986-12-09 | |
US939854 | 1986-12-09 | ||
PCT/US1987/003249 WO1988004237A1 (en) | 1986-12-09 | 1987-12-07 | Thermal imaging medium |
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EP0349532A1 EP0349532A1 (de) | 1990-01-10 |
EP0349532B1 true EP0349532B1 (de) | 1993-11-24 |
EP0349532B2 EP0349532B2 (de) | 2000-07-26 |
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EP88900435A Expired - Lifetime EP0349532B2 (de) | 1986-12-09 | 1987-12-07 | Thermisches aufzeichnungsmittel |
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US (1) | US6245479B1 (de) |
EP (1) | EP0349532B2 (de) |
JP (1) | JP2694928B2 (de) |
KR (2) | KR950008182B1 (de) |
AT (1) | ATE97613T1 (de) |
AU (1) | AU602747B2 (de) |
CA (1) | CA1326400C (de) |
DE (1) | DE3788284T3 (de) |
DK (1) | DK442488A (de) |
FI (1) | FI94108C (de) |
NO (1) | NO302222B1 (de) |
WO (1) | WO1988004237A1 (de) |
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US5231190A (en) | 1991-05-06 | 1993-07-27 | Polaroid Corporation | Squarylium compounds, and processes and intermediates for the synthesis of these compounds |
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-
1987
- 1987-12-07 EP EP88900435A patent/EP0349532B2/de not_active Expired - Lifetime
- 1987-12-07 KR KR1019880700952A patent/KR950008182B1/ko not_active IP Right Cessation
- 1987-12-07 AT AT88900435T patent/ATE97613T1/de not_active IP Right Cessation
- 1987-12-07 AU AU10566/88A patent/AU602747B2/en not_active Ceased
- 1987-12-07 WO PCT/US1987/003249 patent/WO1988004237A1/en active IP Right Grant
- 1987-12-07 JP JP63500720A patent/JP2694928B2/ja not_active Expired - Fee Related
- 1987-12-07 DE DE3788284T patent/DE3788284T3/de not_active Expired - Fee Related
- 1987-12-08 CA CA000553744A patent/CA1326400C/en not_active Expired - Fee Related
-
1988
- 1988-07-29 NO NO883378A patent/NO302222B1/no not_active IP Right Cessation
- 1988-08-08 DK DK442488A patent/DK442488A/da not_active Application Discontinuation
- 1988-08-19 FI FI883863A patent/FI94108C/fi not_active IP Right Cessation
- 1988-12-07 KR KR1019870700952A patent/KR897000476A/ko unknown
-
1999
- 1999-08-09 US US09/370,284 patent/US6245479B1/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
FI883863A (fi) | 1988-08-19 |
ATE97613T1 (de) | 1993-12-15 |
EP0349532B2 (de) | 2000-07-26 |
FI883863A0 (fi) | 1988-08-19 |
JPH02501552A (ja) | 1990-05-31 |
NO883378L (no) | 1988-07-29 |
KR897000476A (ko) | 1989-04-25 |
DE3788284D1 (de) | 1994-01-05 |
WO1988004237A1 (en) | 1988-06-16 |
EP0349532A1 (de) | 1990-01-10 |
AU602747B2 (en) | 1990-10-25 |
FI94108C (fi) | 1995-07-25 |
DE3788284T3 (de) | 2000-10-12 |
KR950008182B1 (ko) | 1995-07-26 |
JP2694928B2 (ja) | 1997-12-24 |
NO883378D0 (no) | 1988-07-29 |
CA1326400C (en) | 1994-01-25 |
FI94108B (fi) | 1995-04-13 |
AU1056688A (en) | 1988-06-30 |
US6245479B1 (en) | 2001-06-12 |
DE3788284T2 (de) | 1994-03-31 |
DK442488A (da) | 1988-10-07 |
DK442488D0 (da) | 1988-08-08 |
NO302222B1 (no) | 1998-02-09 |
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